Medical writing

Expert advice on how to write and edit scientific and medical texts, technical documents and those documents needed for regulatory submission

This course will take participants through all of the necessary steps to obtain marketing authorisation for a feed additive in the European Union.

Book by 10 Apr to save
£200 / €280 / $312

Success in the pharmaceutical industry depends on the speed and efficiency of new drug approvals and the quality of documentation submitted to the regulatory authorities. This intensive practical medical writing course will benefit participants by enabling them to achieve this standard.

Successful Medical Writing

18-20 May 2020

Also on: 5 Oct 2020

Book by 3 Apr to save
£300 / €420 / $468

Presentations will cover the regulatory framework, pharmaceutical, toxicological and pharmacological data, safety risk assessments, pre-clinical and clinical data, Detailed and Critical Summaries and regulatory submissions

Veterinary Pharmaceutical Submissions in the EU

24-25 Mar 2020

Also on: 18 Nov 2020

This practical four day course provides a comprehensive understanding of a veterinary medicine development in the EU and USA.

Book by 10 Apr to save
£400 / €560 / $624